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Hangzhou Jimushi Meditech Co., Ltd.

FDA Regulatory Profile

Hangzhou Jimushi Meditech Co., Ltd. appears in FDA public data with 0 recalls, 3 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 24, 2026.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K260394Hydrophilic coated intermittent nalaton catheter for single use-ready to use (NCR)June 24, 2026
K222677Intermittent nelaton catheter for single useApril 5, 2023
K200134Jimushi Sterile Urethral Catheter for single useJune 1, 2020

FDA data resources